Clearance Summary
L10 LED Light Source with AIM, L11 LED Light Source with AIM, AIM SafeLight Cable received FDA 510(k) clearance under submission number K192292, sponsored by Stryker. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2019-11-19.
- Submission: K192292
- Applicant / Sponsor: Stryker
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2019-11-19
Classification & Regulation
This clearance is catalogued under FDA product code OWN and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.